Blue_DNA_ACTGIn California, one of the state’s biggest health care providers has teamed up with one of its most important research centers to open a powerful new genetic biobank. Kaiser Permanente and the University of California, San Francisco will study the genomes of more than 100,000 Kaiser members who donated their DNA, funding the work with a $25 million grant from the National Institutes of Health.

Biobanks aren’t new, and some, such as Great Britain’s UK Biobank, are larger. But the new biobank is still noteworthy, both for its ambitions and the challenges it will face. If you are thinking about joining a biobank or genetic research project, you’ll want to pay attention to what is happening with this one.

With its focuses on Kaiser members, researchers will have access to participants’ health information. Since most common health conditions arise from a combination of genetics and “environment” (science-speak for non-genetic factors such as food choices, exercise habits, and air quality), being able to blend genetic information with health records is a coveted prize to many researchers.  The average age of biobank participants is 65, allowing researchers to look at genetics and health outcomes over a longer span of time. Diseases of aging, such as heart disease, will be a key focus of the project.

But this won’t be easy. It’s notoriously difficult to tease clear answers out of a thicket of thousands of DNA profiles and personal health records. The project has two years to pull all that information together in a usable way.

As with other reputable biobanks, participation in the Kaiser biobank is voluntary. If you are thinking about joining a biobank or other genetic research project, you can find some general information in Chapter 2 of our book. You’ll find specific information on protecting your privacy in Chapter 8.

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"As you read these pages, I hope you will be inspired to explore how you might use genetic information to improve your own health."
- Catherine Wicklund, MS, CGC
President, National Society of Genetic Counselors, 2007
from her foreword to The Genome Book

About the authors

April Lynch is an author whose work focuses on health and genetics. As an award-winning journalist, she directed coverage of science, health, and medicine for The San Jose Mercury News, Silicon Valley's leading newspaper. She has also written for a variety of other organizations, including leading university textbook publisher Pearson Education and genomics firm Navigenics. Her work on the book and this blog reflects her views, and not those of any employer or organization.


Vickie Venne, MS, CGC, is celebrating 30 years as a genetic counselor. She worked in prenatal, pediatric, and laboratory settings before joining the Hunstman Cancer Institute at the University of Utah. In addition to caring for patients, she has taught for the California Department of Education and the University of Utah's graduate program in genetic counseling. She has also served as president of the National Society of Genetic Counselors and the local affiliate of the Susan G. Komen Breast Cancer Foundation. Her work on the book and this blog reflects her views, and not those of any employer or organization.